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The courses will provide entry-level clinical laboratory experiences in the areas of Microbiology and Immunohematology. The courses will provide entry-level clinical laboratory experiences in the areas of Microbiology and Immunohematology.
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Requirements: High school diploma and a graduate of accredited Physician Assistant program with state accreditation based on certifying exam Strong communication skills and the ability to work well with a team in a fast-paced environment Previous clinical experience is preferred Powered by JazzHR.
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Submit your online application so it is on file for the hiring manager, then come by our open house and meet our great team! Assist with Staff Management and provide backup support to Club Manager as needed.
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Continuing Education Allowance far exceeding industry standards 2 Paid Continuing Education Days Monthly Onsite Education Clinical and Leadership Mentorship Program MedBridge Subscription Clinical Ladder for Advancement Opportunity inclusive of Leadership Advancement Opportunity to mentor students as a Clinical Instructor Salary Range - $95,000 - $105,000 / year If this sounds like the perfect opportunity for you, send in your resume.
$95,000 - $105,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Professional Project Management and Agile certification (e.g. PMP, PMI-ACP, Scrum Master) Professional Project Management and Agile certification (e.g. PMP, PMI-ACP, Scrum Master) Manage project financials, including budgeting, forecasting, and financial reporting, ensuring alignment with business objectives.
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In terms of plasmid service, GenScript ProBio supports the most clinical approvals for CGT drugs including mRNA vaccines, CAR-T in China. GenScript ProBio’s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
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2 current clinical references. Our Client is currently seeking Med Surg Tele for positions in Somerville, NJ for a 3x12 Nights shift. Refer a friend and earn extra cash. The ideal candidate will possess a current NJ license or Compact license Depending on the state.
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To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as a Director, Business Development remotely from a home-based office in the USA in accordance with our Work from Home policies or in our Bridgewater, New Jersey, USA on-site location.
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Position Summary: The Director, Clinical Systems and TMF Operations is a member of the Clinical Business Operations team within the Development Operations organization and is responsible to provide strategic leadership and oversight of Trial Master File (TMF) Operations, Records Management, and Clinical Systems & Technology (CS+T) utilized across clinical programs.
$250,800 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Responsibilities: Provides clinical, scientific, and strategic oversight of projects within our development portfolioProvides in-house expertise on clinical, regulatory, and strategic projectsMay supervise 1-3 medical directors at the associate director, director or sr.
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The New Jersey Judiciary consists of: the Supreme Court, the Superior Court including the Appellate Division and the Trial Court of the 15 vicinages in New Jersey, the Tax Court and the Municipal Court System.
$113,982.01 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Bachelor degree plus minimum 6 years or Master degree plus minimum 4 years of experience or PhD plus 1 year of experience in Pharmaceutics, Chemistry, Biomedical Engineering, Chemical Engineering, or related field with a strong background in nanoparticle-based formulation development & analytical characterization.
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Initial draft authoring of scientific content for Common Technical Document (CTD) Quality sections and responses to health authority questions aligned with regulatory strategy for cell therapy clinical CMC regulatory submissions based on high quality technical reports.
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Master's degree in biology, Cell Biology, Molecular Biology, Immunology, or related discipline, or bachelor's degree with at least 2 years of pharmaceutical experience.
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Hands-on experience in Master Data Management (MDM) Helps clients better manage their customer master data (doctors and hospitals) to improve data quality. Data Steward performs data stewardship operations using Veeva Network, Veeva Open Data and Veeva CRM.
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clinical trial master file jobs Title: trial master in Raritan, NJ
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